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m-Chloroperbenzoic acid → 4-(diethylphosphonomethyl)pyridine-N-oxide

HRID 1198870
Notes
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Reaction equation

HRID 1198870 reaction equation
[CH2:1]([O:3][P:4]([CH2:9][C:10]1[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=1)([O:6][CH2:7][CH3:8])=[O:5])[CH3:2].ClC1C=CC=C(C(OO)=[O:24])C=1>C(Cl)(Cl)Cl>[CH2:1]([O:3][P:4]([CH2:9][C:10]1[CH:11]=[CH:12][N+:13]([O-:24])=[CH:14][CH:15]=1)([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 10078602Diethyl (pyridin-4-ylmethyl)phosphonate

Product 1

HCID 145414374-(diethylphosphonomethyl)pyridine-N-oxide

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

A mixture of 2.2 g of 4-(diethylphosphonomethyl)pyridine [Roczniki Chem. 38, (4), 625 (1964); Chem. Abst. 61, 10703], 2.2 g of m-chloroperbenzoic acid and 30 ml of chloroform is stirred at room temperature for 16 hours. The solvent is removed in vacuo and water is added. After washing the aqueous layer with ether, the water is removed in vacuo to afford 4-(diethylphosphonomethyl)pyridine-N-oxide.

Workup

  1. customThe solvent is removed in vacuo and water
  2. additionis added
  3. washAfter washing the aqueous layer with ether
  4. customthe water is removed in vacuo

Sources & evidence

ORD record
ord-dab61b71098d40a6951f62db385cd1f4
Source dataset
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04898854

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes